Canonical Allele Identifier: PA2827301218
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1445464
ClinVar RCV Id: RCV001985055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Ile1187Thr
CA346819287
NM_001330086.2:c.3560T>C